|
OMIM |
Link |
Information gain |
01 |
|
splenic hypoplasia
|
[NCBI]
|
0.00213636
|
|
|
adrenal unresponsiveness to acth
|
[NCBI]
|
0.000991404
|
|
|
ALD
|
[NCBI]
|
0.000947767
|
|
|
AIMAH
|
[NCBI]
|
0.000682059
|
|
|
wolman disease
|
[NCBI]
|
0.000257217
|
|
|
AAA
|
[NCBI]
|
0.000229013
|
|
|
AHC
|
[NCBI]
|
0.000214257
|
|
|
ABCD1
|
[NCBI]
|
0.000179805
|
|
|
CRH
|
[NCBI]
|
0.000173083
|
|
|
lipoid congenital adrenal hyperplasia
|
[NCBI]
|
0.000152266
|
|
|
ectodermal dysplasia with adrenal cyst
|
[NCBI]
|
0.000124742
|
|
|
AAAS
|
[NCBI]
|
0.000116607
|
|
|
scalp-ear-nipple syndrome
|
[NCBI]
|
8.42118e-05
|
|
|
GCCD1
|
[NCBI]
|
6.90246e-05
|
|
|
BWS
|
[NCBI]
|
5.5766e-05
|
|
|
NOV
|
[NCBI]
|
5.06713e-05
|
|
|
CNC1
|
[NCBI]
|
4.92209e-05
|
|
|
CRHR1
|
[NCBI]
|
4.76717e-05
|
|
|
GK
|
[NCBI]
|
4.47134e-05
|
|
|
adrenoleukodystrophy, autosomal neonatal form
|
[NCBI]
|
4.47034e-05
|
|
|
PRKAR1A
|
[NCBI]
|
4.24411e-05
|
|
|
NR5A1
|
[NCBI]
|
3.97895e-05
|
|
|
NR0B1
|
[NCBI]
|
3.70976e-05
|
|
|
protein c deficiency, congenital thrombotic disease due to
|
[NCBI]
|
3.06657e-05
|
|
|
STAR
|
[NCBI]
|
2.83844e-05
|
|
|
MEN1
|
[NCBI]
|
2.45987e-05
|
|
|
ADM
|
[NCBI]
|
2.19729e-05
|
|
|
SLE
|
[NCBI]
|
2.01365e-05
|
|
|
PYY
|
[NCBI]
|
1.98878e-05
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
1.97457e-05
|
|
|
GIP
|
[NCBI]
|
1.72643e-05
|
|
|
POMC
|
[NCBI]
|
1.52829e-05
|
|
|
AVP
|
[NCBI]
|
1.38952e-05
|
|
|
FMF
|
[NCBI]
|
8.67371e-06
|
|
|
CD
|
[NCBI]
|
7.9166e-06
|
|
|
PRL
|
[NCBI]
|
7.66833e-06
|
|
|
NPPA
|
[NCBI]
|
6.87446e-06
|
|
|
VIP
|
[NCBI]
|
6.24423e-06
|
|
|
VEGF
|
[NCBI]
|
3.51386e-06
|
|
|
EGF
|
[NCBI]
|
1.02083e-07
|
|
|
EGFR
|
[NCBI]
|
5.01958e-08
|
|